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利用高速原子力显微镜直接观察DNA折纸框架中含G-四链体/i-基序序列的双链DNA的形成和解离

Direct Observation of the Formation and Dissociation of Double-Stranded DNA Containing G-Quadruplex/i-Motif Sequences in the DNA Origami Frame Using High-Speed AFM.

作者信息

Endo Masayuki, Xing Xiwen, Sugiyama Hiroshi

机构信息

Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto, Japan.

Institute for Integrated Cell-Material Sciences, Kyoto University, Kyoto, Japan.

出版信息

Methods Mol Biol. 2019;2035:299-308. doi: 10.1007/978-1-4939-9666-7_17.

Abstract

We demonstrate the single-molecule operation and observation of the formation and resolution of double-stranded DNA (dsDNA) containing G-quadruplex (GQ)- and counterpart i-motif-forming sequences in the DNA nanostructure. Sequential manipulation of DNA strands in the DNA frame was performed to prepare a topologically controlled GQ/i-motif dsDNA. Using the strand displacement and the addition and removal of K, the topologically controlled GQ/i-motif dsDNA in the DNA frame was obtained in high yield. The dsDNA was resolved into the single-stranded DNA, GQ, and i-motif by the addition of K and operation under acidic conditions. The dissociation of the dsDNA under the GQ and i-motif formation conditions was monitored by high-speed atomic force microscopy. The results indicate that the dsDNA containing the GQ- and i-motif sequence is effectively dissolved when the duplex is helically loosened in the DNA nanoscaffold.

摘要

我们展示了在DNA纳米结构中对包含G-四链体(GQ)和对应i-基序形成序列的双链DNA(dsDNA)进行单分子操作以及对其形成和解析过程的观察。在DNA框架中对DNA链进行顺序操作,以制备拓扑结构可控的GQ/i-基序dsDNA。通过链置换以及添加和去除钾离子,以高产率获得了DNA框架中拓扑结构可控的GQ/i-基序dsDNA。通过添加钾离子并在酸性条件下操作,dsDNA被解析为单链DNA、GQ和i-基序。利用高速原子力显微镜监测了在GQ和i-基序形成条件下dsDNA的解离情况。结果表明,当双链在DNA纳米支架中螺旋松弛时,包含GQ和i-基序序列的dsDNA能有效溶解。

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